跳至主要内容
临床试验/EUCTR2018-002144-85-IT
EUCTR2018-002144-85-IT进行中(未招募)1 期

A 52-Week, open-label, single-arm study to evaluate the safety and tolerability of 24-hour daily exposure of continuous subcutaneous infusion of ABBV-951 in subjects with Parkinson's disease - Galliarde

ABBVIE DEUTSCHLAND GMBH & CO. KG0 个研究点目标入组 130 人开始时间: 2021年6月15日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
130

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Adult male or female subjects, 30 years of age or older at the time of screening, with a diagnosis of idiopathic PD that is levodopa-responsive
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 65
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 65

排除标准

  • Subjects judged by the investigator to be adequately controlled by current therapy, that don't have recognizable/identifiable Off and On states (motor fluctuations), and have less than 2.5 hours of Off time per day.

研究者

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